Hello. I will do Colony Formation analysis for my master's thesis.

I'm trying to create a standard protocol for Clonogenic assay or colony formation assay.

I would appreciate it if you could share your knowledge on this subject.

Thanks in advance.

Important questions:

  • What to use when fixing cells before imaging? (such as formaldehyde, praformaldehyde or methanol)
  • Is there a specific temperature for the solution?
  • How long is the incubation period of the solution?
  • Are you viewing the fixed cells with a microscope or a special device?
  • Similar questions and discussions